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The Educational ARDS Diagnosis Study

Randomized Educational ARDS Diagnosis Study (READS)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02054611
Acronym
READS
Enrollment
600
Registered
2014-02-04
Start date
2014-02-28
Completion date
2014-09-30
Last updated
2014-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ARDS

Keywords

ARDS, Chest radiographs, Vignettes, Online educational video

Brief summary

Without rigorous, high-quality training materials, the results of the LUNG-SAFE study examining the global incidence and outcomes of severe lung failure (acute respiratory distress syndrome \[ARDS\]) could be confused by either under-recognition of patients with, or misclassification of patients without, ARDS. This problem has been previously identified with the use of the prior ARDS definitions, particularly in patients with milder severity of illness. Importantly, the chest x-ray criteria in the ARDS definition has demonstrated only moderate reliability when applied by experts, although this can be improved through the use of training radiographs (as will be used in this educational module). The investigators hypothesize that the training from the educational module will allow more accurate diagnosis of ARDS by data collectors/study coordinators participating in the LUNG-SAFE study.

Detailed description

In this LUNG-SAFE sub-study, the investigators will evaluate the effect of a brief online educational module on correctly identifying patients (i.e., standardized cases) with ARDS according to the Berlin Definition. The investigators hypothesize that the training from the educational module will allow more accurate diagnosis of ARDS according to the Berlin Definition by participating data collectors/study coordinators. Data collectors and study coordinators from ICUs participating in LUNG-SAFE would be randomized (by simple random number generator) to one of the following online educational streams: 1. Educational module completion followed by evaluation 2. Evaluation followed by educational module completion Limited demographic data will be collected from the respondents, along with their responses to the 15 multiple choice test questions. Time spent viewing the educational module will also be collected.

Interventions

OTHEROnline Educational Module

A descriptive video detailing the diagnosis of ARDS according to the Berlin Definition, along with online educational materials available for review.

OTHEREvaluation First (Placebo)

The respondents will view the descriptive video detailing the diagnosis of ARDS according to the Berlin Definition, along with online educational materials available for review only after they have completed the evaluation.

Sponsors

Unity Health Toronto
CollaboratorOTHER
Sunnybrook Health Sciences Centre
CollaboratorOTHER
University of Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Study coordinators/data collectors for the LUNG-SAFE study

Exclusion criteria

* No informed consent to participate

Design outcomes

Primary

MeasureTime frameDescription
ARDS Diagnosisup to 4 weeksThe number of correct responses to the evaluation component (15 multiple choice questions) of the educational module (in aggregate).

Secondary

MeasureTime frameDescription
ARDS Diagnosisup to 4 weeksNumber of correct responses to the evaluation component of the educational modules, separated by question type (vignettes vs. chest x-rays)
Timeup to 4 weeksAmount of time spent completing the educational module

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026